A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398097



Internal ID21055650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86018201..86062700hg38UCSC Ensembl
chr5:85314019..85358518hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3844500
hg1944500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5801n223
Supporting Variantsnssv18214300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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